The following data is part of a premarket notification filed by Ditron Precision Ltd with the FDA for Dental Implants And Abutments.
| Device ID | K161497 |
| 510k Number | K161497 |
| Device Name: | Dental Implants And Abutments |
| Classification | Implant, Endosseous, Root-form |
| Applicant | Ditron Precision Ltd Haofe 2 St., P.O Box 5010 Netanya, IL 78150 |
| Contact | Moshe Orlev |
| Correspondent | Tali Hazan Talmed Ltd Ramot Naftali, M.P Upper Galillee Ramot Naftali, IL 13830000 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-06-01 |
| Decision Date | 2016-10-28 |
| Summary: | summary |